Compositions and methods for converting hazardous waste glass into non-hazardous products

ABSTRACT

The present invention provides compositions and methods for converting hazardous waste glass into safe and usable material. In particular, the present invention provides compositions and methods for producing ceramic products from toxic-metal-containing waste glass, thereby safely encapsulating the metals and other hazardous components within the ceramic products.

CROSS-REFERENCE TO RELATED APPLICATION

The present application claims priority to pending U.S. ProvisionalPatent Application No. 61/328,845, filed Apr. 28, 2010, the contents ofwhich are incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention provides compositions and methods for convertinghazardous waste glass into safe and usable material. In particular, thepresent invention provides compositions and methods for producingceramic products from toxic-metal-containing waste glass, thereby safelyencapsulating metals and other hazardous components within the ceramicproducts.

BACKGROUND

A cathode ray tube (CRT) is a video display component of manytelevisions and computer monitors. A typical CRT weighs between 15 and90 pounds and contains significant quantities of lead, barium, and otherelements that are added to the specialized CRT glass, in some cases toprotect the user from x-rays generated within the operating CRT. CRTglass is comprised of up to 25% lead oxide (PbO). The major hazardouscomponents of CRTs are lead and barium found in the glass and sealcomponents. The lead content of a typical color CRT is about 2.5 lb.Most of the lead is found in the funnel glass and the face plate-funnelseal since most manufacturers have eliminated lead from the panel glassand the neck glass represents a relatively small part of a typical tube.The glass for the funnel and neck sections are characterized by highlevels of lead oxide and the glass for display panel typically containshigh levels of barium oxide [2-4].

A major obstacle to reuse and disposal is the fact that the leachabilityof lead causes the CRT components to fail the EPA TCLP leaching test[5]. Because of the high lead content, CRT glass is no longer to bedisposed of in the trash or in municipal landfills. While CRT glass maybe disposed of in hazardous waste landfills, this is a costly option andrecycling is the preferred management option for end-of-life CRTs.Currently, CRTs are recycled through a process which involves extractingthe lead using a smelting process. The smelting process is costly andresults in high levels of air and water pollution. Cathode ray tubespresently have a negative value due to the difficulty and hazardsassociated with recycling and/or disposing of them. Similar difficultiesin disposal arise with other glasses containing hazardous materials,such as fluorescent light bulbs.

Methods have been developed for converting waste glass into ceramicproducts. However, established methods for conversion of waste glassinto other useful materials (e.g., ceramics) do not address thehazardous components of CRT glass and other hazardous waste glasses. Thefield currently lacks suitable techniques for the safe encapsulation ofheavy metals and other hazardous compounds into products and/ormaterials made from CRT glass and other hazardous waste glass.

SUMMARY OF THE INVENTION

Experiments conducted during the course of developing embodiments forthe present invention demonstrated production of ceramic products fromtoxic-metal-containing waste glass, wherein the ceramic products safelyencapsulate the metals and other hazardous components. Accordingly, thepresent invention provides compositions and methods for convertinghazardous waste glass into safe and usable material. In particular, thepresent invention provides compositions and methods for producingceramic products from toxic-metal-containing waste glass, thereby safelyencapsulating metals and other hazardous components within the ceramicproducts.

In certain embodiments, the present invention provides methods forproducing a ceramic article from hazardous waste glass comprising: (a)mixing the hazardous waste glass with a filler and a non-aqueous binder,(b) pressing the mixture to produce a green article, and (c) firing thegreen article to produce a ceramic article. In some embodiments, thehazardous waste glass comprises greater than 1% lead (e.g., 1.01% Pb, 2%Pb, 3% Pb, 4% Pb, 5% Pb, 10% Pb, 20% Pb, 30% Pb, 40% Pb, 50% Pb, etc.).In some embodiments, the hazardous waste glass comprises greater than 1%barium (e.g., 1.01% Ba, 2% Ba, 3% Ba, 4% Ba, 5% Ba, 10% Ba, 20% Ba, 30%Ba, 40% Ba, 50% Ba, etc.). In some embodiments, the hazardous wasteglass comprises CRT glass. In some embodiments, the hazardous wasteglass comprises fluorescent light glass. In some embodiments, the fillercomprises alumina, magnesium silicate (e.g., Talc), and/or bentonite(e.g., clay). In some embodiments, the choice of filler is dependentupon the ultimate desired use of the ceramic article (e.g.,indoor/outdoor use for the ceramic article) (e.g, use of magnesiumsilicate as a filler for outdoor ceramic articles as magnesium silicatewithstands temperature changes expansion and contraction). In someembodiments, the non-aqueous binder comprises polyvinyl alcohol. In someembodiments, the non-aqueous binder prevents the emission ofhydrocarbons during, for example, a firing stage (e.g., wherenon-aqueous binder is sodium silicate). In some embodiments, pressingcomprises dry pressing. In some embodiments, pressing comprises placingthe mixture under pressure of at least 200 kg/cm². In some embodiments,pressing comprises placing the mixture under pressure of about 400kg/cm². In some embodiments, firing comprises heating the green articleto at least 500° C. In some embodiments, firing comprises heating thegreen article to a temperature less than 1000° C. In some embodiments,firing comprises heating the green article to at least 650° C. In someembodiments, the firing comprises heating the green article to atemperature less than 815° C.

In certain embodiments, the present invention provides methods ofproducing ceramic articles from hazardous waste glass comprising: (a)mixing hazardous waste glass with a filler, and a plastic material, (b)mixing the hazardous waste glass, filler, and plastic material mixturewith a non-aqueous binder to produce a batch mixture, (c) pressing thebatch mixture to produce a green article, (d) drying the green article,and (e) firing the green article to produce a ceramic article. In someembodiments, the hazardous waste glass comprises greater than 1% lead.In some embodiments, the hazardous waste glass comprises CRT glass. Insome embodiments, the hazardous waste glass comprises fluorescent lightglass. In some embodiments, the filler comprises alumina, magnesiumsilicate, and/or bentonite. In some embodiments, the plastic materialcomprises clay. In some embodiments, the non-aqueous binder comprisespolyvinyl alcohol or sodium silicate (e.g., so as to prevent theemission of hydrocarbons during, for example, a firing stage). In someembodiments, mixing the hazardous waste glass with the filler andplastic material comprises wet stirring followed by drying. In someembodiments, pressing comprises placing the mixture under pressure of atleast 200 kg/cm². In some embodiments, pressing comprises placing themixture under pressure of about 400 kg/cm². In some embodiments, firingcomprises heating the green article to at least 500° C. In someembodiments, firing comprises heating the green article to a temperatureless than 1400° C. In some embodiments, firing comprises heating saidgreen article to at least 650° C. In some embodiments, firing comprisesheating the green article to a temperature less than 1250° C. In someembodiments, the method further comprises a step between steps (a) and(b) of sieving the batch mixture through a first mesh. In someembodiments, the first mesh comprises a 50-150 mesh. In someembodiments, the method further comprises a step between steps (b) and(c) of sieving the batch mixture through a second mesh. In someembodiments, the second mesh comprises a 10-40 mesh. In someembodiments, the second mesh comprises about 20 mesh.

In certain embodiments, the present invention provides methods forrecycling hazardous waste glass comprising: (a) providing hazardouswaste glass as a starting material, and (b) producing a ceramic articlefrom the hazardous waste glass, wherein the ceramic article safelyencapsulates the hazardous components of the hazardous waste glass. Insome embodiments, the hazardous waste glass comprises significantquantities of toxic and/or heavy metals. In some embodiments, theceramic article meets EPA standards for toxicity and leaching of toxicand/or heavy metals. In some embodiments, the ceramic article exhibitslead leachate concentrations of less than 5 ppm. In some embodiments,the hazardous waste glass comprises greater than 1% lead. In someembodiments, the hazardous waste glass comprises greater than 5% lead.In some embodiments, the hazardous waste glass comprises greater than20% lead. In some embodiments, the ceramic article exhibits bariumleachate concentrations of less than 100 ppm. In some embodiments, theceramic article exhibits barium leachate concentrations of less than 10ppm. In some embodiments, the hazardous waste glass comprises greaterthan 1% barium. In some embodiments, the hazardous waste glass comprisesgreater than 5% barium. In some embodiments, the hazardous waste glasscomprises greater than 20% barium. In some embodiments, the hazardouswaste glass comprises CRT glass. In some embodiments, the hazardouswaste glass comprises fluorescent light glass.

In certain embodiments, the present invention provides ceramic articlescomprising hazardous waste glass. In some embodiments, the ceramicarticles comprise a ceramic tile. In some embodiments, the ceramic tilecomprises a floor tile. In some embodiments, the ceramic tile comprisesa wall tile. In some embodiments, the hazardous waste glass comprisesCRT glass. In some embodiments, the hazardous waste glass comprisesfluorescent light glass. In some embodiments, the ceramic articlecomprises greater than 40% hazardous waste glass. In some embodiments,the ceramic article comprises greater than 60% hazardous waste glass. Insome embodiments, the ceramic article comprises greater than 80%hazardous waste glass. In some embodiments, the ceramic articlecomprises greater than 90% hazardous waste glass. In some embodiments,the ceramic article comprises significant quantities of heavy and/ortoxic metals. In some embodiments, the ceramic article meets EPAstandards for toxicity and leaching of toxic and/or heavy metals. Insome embodiments, the ceramic article exhibits lead leachateconcentrations of less than 5 ppm. In some embodiments, the hazardouswaste glass comprises greater than 1% lead. In some embodiments, thehazardous waste glass comprises greater than 5% lead. In someembodiments, the hazardous waste glass comprises greater than 20% lead.In some embodiments, the ceramic article exhibits barium leachateconcentrations of less than 100 ppm. In some embodiments, the ceramicarticle exhibits barium leachate concentrations of less than 10 ppm. Insome embodiments, the hazardous waste glass comprises greater than 1%barium. In some embodiments, the hazardous waste glass comprises greaterthan 5% barium. In some embodiments, the hazardous waste glass comprisesgreater than 20% barium.

DESCRIPTION OF THE FIGURES

FIG. 1 shows a lab-scale fabrication process for ceramic tile utilizingCRT glass.

FIG. 2 shows images of fired tiles made from CRT glass

FIG. 3 shows backscattered SEM images of sintered ceramic tile from CRTglass: (a) 40 wt % loading, (b) 60 wt % loading. The microstructureshows the uniform distribution of filler minerals; needle-shapedhigh-barium aluminosilicate phases have been formed surrounding thefiller giving a porphyritic texture. The concentration of fillerminerals is reduced by the higher loading, and a second phase is beingdeveloped surrounding the filler. This acicular type of phase would forma netlike structure inside the tile body, which enhances strength.

FIG. 4 shows XRD pattern identifying phases present in fired tiles.

FIG. 5 shows XRD patterns of tiles made from CRT glass before (top) andafter (bottom) firing.

FIG. 6 shows a flow chart for the production-scale fabrication ofsingle-fired wall tile.

FIG. 7 shows a flow chart for the production-scale fabrication ofdouble-fired wall tile.

DEFINITIONS

To facilitate an understanding of the present invention, a number ofterms and phrases are defined below:

As used herein, the term “waste glass” refers to any unwanted orunusable glass products or materials including post-consumer glass,industrial waste glass, production defect glass, and/or byproduct glass.“Waste glass” may comprise any level of hazardous materials, includingbeing devoid of any hazardous materials, as in “non-hazardous wasteglass.”

As used herein, the term “hazardous waste glass” refers to waste glasswhich contains hazardous materials (e.g., heavy metals, toxic metals,etc.) as a component of the glass. Disposal of “hazardous waste glass”is complicated by the need to safely and efficiently deal with thehazardous materials within the glass.

As used herein, the term “heavy metals” refers to the subset of elementsthat exhibit metallic properties, which would mainly include thetransition metals and some metalloids. As used herein, the term “heavymetals” generally refers to a subset of elements which have been deemedharmful, hazardous, polluting, or dangerous to health or theenvironment. “Heavy metals” include mercury, arsenic, cadmium, cobalt,chromium, copper, manganese, nickel, lead, tin and thallium. Some “heavymetals” are actually necessary for humans in minute amounts (Co, Cu, Cr,Ni), while others are carcinogenic or toxic, affecting, among others,the central nervous system (Hg, Pb, As); the kidneys or liver (Hg, Pb,Cd, Cu); or skin, bones, or teeth (Ni, Cd, Cu, Cr).

As used herein, the term “toxic metal” refers to metal elements thatform poisonous soluble compounds and either have no biological role(e.g., are not essential minerals), are in the wrong form, or arepresent in an abnormally high, toxic doses. “Toxic metals” include:antimony, barium, beryllium, aluminum, cadmium, lead, mercury, osmium,thallium, and vanadium. As used herein, the term “starting material,”also known as “input material,” refers to materials and components usedto produce ceramic products and/or materials. Starting materialsinclude, for example flux (e.g., hazardous waste glass (e.g., CRT glass,fluorescent glass, etc.)), filler (e.g., alumina, magnesium silicate,and/or bentonite), and plastic material (e.g., clay). Starting materialsmay be in a raw or unmanipulated form (e.g., glass within a CRT), or ina processed form (e.g., ground and sieved CRT glass).

As used herein, the term “raw material” refers to a starting material inan unmanipulated or unrefined form. “Raw material” may be ready for usein methods of the present invention or may require one or morepre-processing steps. For example, hazardous waste glass is a “rawmaterial” that may require grinding or removal of additional parts priorto use in methods of the present invention. Pre-processing of “rawmaterials” is within the scope of the methods of the present invention,but is not a required element.

As used herein, the term “batch mixture” refers to a mixture of startingmaterials being processed according to methods of the present invention.“Batch mixture” refers to materials during any step of processingfollowing mixing of starting materials and prior to the finishedproduct. For example, “batch mixture” may comprise flux (e.g., hazardouswaste glass (e.g., CRT glass, fluorescent glass, etc.)), filler (e.g.,alumina, magnesium silicate, and/or bentonite), and plastic material(e.g., clay); flux (e.g., hazardous waste glass (e.g., CRT glass,fluorescent glass, etc.)), filler (e.g., alumina, magnesium silicate,and/or bentonite), plastic material (e.g., clay), and binder (e.g.,polyvinyl alcohol or sodium silicate); flux (e.g., hazardous waste glass(e.g., CRT glass, fluorescent glass, etc.)) and filler (e.g., alumina,magnesium silicate, and/or bentonite); or flux (e.g., hazardous wasteglass (e.g., CRT glass, fluorescent glass, etc.)), filler (e.g.,alumina, magnesium silicate, and/or bentonite), and binder (e.g.,polyvinyl alcohol and/or sodium silicate).

As used herein, the term “green article” refers to an article in anunfired or pre-fired state. A “green article” may comprise a greenmaterial and/or a green product. A batch mixture which has been mixed,but not yet fired is referred to as a “green article.” A “green article”typically refers to an article which has undergone most or allprocessing steps, short of firing.

As used herein, the term “plastic” refers to a material that ismalleable or capable of being shaped and formed (e.g., clay). A“plastic” material may be of natural or synthetic origins, and does notnecessarily refer to a synthetic or semisynthetic organic polymermaterial.

DETAILED DESCRIPTION OF THE INVENTION

Experiments conducted during the course of developing embodiments forthe present invention demonstrated production of ceramic products fromtoxic-metal-containing waste glass, wherein the ceramic produces safelyencapsulate the metals and other hazardous components.

Accordingly, the present invention provides compositions, devices,systems, and methods for recycling hazardous waste glass (e.g., heavymetal-containing glass (e.g., lead, barium, etc.)). In particular, thecompositions, devices, systems and methods of the present inventionconvert hazardous waste glass into a material which safely encapsulateshazardous components (e.g., heavy metals, toxic metals, etc.) of thewaste glass within a new material (e.g., ceramic end product). Thepresent invention is not limited to the generation of a particularnon-hazardous material through recycling of hazardous waste glass. Insome embodiments, the non-hazardous material is a ceramic product. Thepresent invention is not limited to a particular type of ceramicproduct. In some embodiments, the present invention providescompositions and methods for the production of ceramic tiles fromhazardous waste glass. In some embodiments, the present inventionprovides compositions and methods for the production of ceramic tilesfrom CRT glass and/or fluorescent light glass. Indeed, in someembodiments, the present invention provides ceramic materials and/orproducts (e.g., ceramic tiles) produced using hazardous waste glass(e.g., CRT glass, fluorescent light glass, etc.) as an input material.

The present invention is not limited to particular compositions,devices, systems, and/or methods for accomplishing such recycling ofhazardous waste glass into a non-hazardous material. For example, thecompositions, systems, devices and methods recycle hazardous waste glasssuch that the inherent hazardous materials are safely encapsulatedwithin a material (e.g., a ceramic end product) incapable of leachinginto the surrounding environment (e.g., air, water, skin, etc.). Asnoted, in some embodiments, the present invention provides compositionsand methods for transforming hazardous and/or potentially hazardouswaste glass into ceramic products (e.g., ceramic tiles) and/or ceramicmaterial safely encapsulating the hazardous materials (e.g., lead,mercury, barium, etc.) within the hazardous waste glass (e.g., thehazardous materials are incapable of leaching from ceramic and/or leachbelow an acceptable threshold of leachability, etc.). In someembodiments, materials and products of the present invention generateend products (e.g., ceramic products) that encapsulate and/or areconfigured to prevent leaching of hazardous materials (e.g., heavymetals, toxic metals, etc.) that would otherwise have to be removedprior to recycling or disposal. As such, the present invention providesa significant improvement over existing recycling technologies renderingend products having unacceptable hazardous waste content.

Accordingly, the present invention provides compositions and methods forconverting hazardous waste glass into safe and usable material. Inparticular, the present invention provides compositions and methods forproducing ceramic products from toxic-metal-containing waste glass,thereby safely encapsulating the metals and other hazardous componentswithin the ceramic products.

The present invention is not limited to particular methods for recyclinghazardous waste glass (e.g., CRT glass, fluorescent light glass, etc.),encapsulating hazardous materials (e.g., heavy metals, toxic metals,etc.), and/or producing ceramic materials and/or products. In someembodiments, the methods produce ceramic materials and/or productsencapsulating hazardous materials (e.g., heavy metals, toxic metals,etc.) and prevent leaching thereof, comprising, for example, mixinginput materials (e.g., flux material (e.g., hazardous waste glass),filler, binder, plastic material), pressing the mixed input materials,and firing the pressed mixed input materials to generate a ceramicproduct that encapsulates hazardous materials.

The present invention is not limited to particular input materials usedin methods for producing ceramic product that encapsulates hazardousmaterials from hazardous waste glass. Examples of input materialsinclude, but are not limited to, flux material (e.g., hazardous wasteglass (e.g., CRT glass, fluorescent light glass, etc.)), filler (e.g.,alumina, magnesium silicate, and/or bentonite), binder (e.g., polyvinylalcohol or sodium silicate) and plastic material (e.g., clay). In someembodiments, the methods use more than one type of input material (e.g.,flux material and binder; flux material and filler; flux material,binder, filler and plastic material).

The present invention is not limited to a particular type and/or kind offlux material. In some embodiments, the flux material compriseshazardous waste glass. The present invention is not limited toparticular types of hazardous waste glass. Examples of hazardous wasteglass include, but are not limited to, CRT glass, fluorescent lightglass, and/or other hazardous waste glass (e.g., glass containingquantities of toxic metals, heavy metals, etc.).

In some embodiments, hazardous waste glass comprises significantquantities of toxic metals, heavy metals, and/or other hazardouscompounds. In some embodiments, hazardous waste glass comprisessignificant quantities of one or more of antimony, barium, beryllium,aluminum, cadmium, lead, mercury, osmium, thallium, and vanadium. Insome embodiments, hazardous waste glass comprises greater than 0.1% lead(e.g., PbO) by weight % (e.g., 0.2% . . . 0.5% . . . 1.0% . . . 2% . . .5% . . . 10% . . . 15% . . . 20% . . . 25% . . . 30% . . . 40% . . . 50%. . . 60% . . . 75% . . . 90% . . . >95%). In some embodiments,hazardous waste glass comprises greater than 0.1% barium (e.g., BaO) byweight % (e.g., 0.2% . . . 0.5% . . . 1.0% . . . 2% . . . 5% . . . 10% .. . 15% . . . 20% . . . 25% . . . 30% . . . 40% . . . 50% . . . 60% . .. 75% . . . 90% . . . >95%). In some embodiments, hazardous waste glasscomprises greater than 0.1% mercury by weight % (e.g., 0.2% . . . 0.5% .. . 1.0% . . . 2% . . . 5% . . . 10% . . . 15% . . . 20% . . . 25% . . .30% . . . 40% . . . 50% . . . 60% . . . 75% . . . 90% . . . >95%). Insome embodiments, hazardous waste glass comprises greater than 0.1%silver by weight % (e.g., 0.2% . . . 0.5% . . . 1.0% . . . 2% . . . 5% .. . 10% . . . 15% . . . 20% . . . 25% . . . 30% . . . 40% . . . 50% . .. 60% . . . 75% . . . 90% . . . >95%). In some embodiments, hazardouswaste glass comprises greater than 0.1% selenium by weight % (e.g., 0.2%. . . 0.5% . . . 1.0% . . . 2% . . . 5% . . . 10% . . . 15% . . . 20% .. . 25% . . . 30% . . . 40% . . . 50% . . . 60% . . . 75% . . . 90% . .. >95%). In some embodiments, hazardous waste glass comprises greaterthan 0.1% toxic metals by weight % (e.g., 0.2% . . . 0.5% . . . 1.0% . .. 2% . . . 5% . . . 10% . . . 15% . . . 20% . . . 25% . . . 30% . . .40% . . . 50% . . . 60% . . . 75% . . . 90% . . . >95%). In someembodiments, hazardous waste glass comprises greater than 0.1% heavymetals by weight % (e.g., 0.2% . . . 0.5% . . . 1.0% . . . 2% . . . 5% .. . 10% . . . 15% . . . 20% . . . 25% . . . 30% . . . 40% . . . 50% . .. 60% . . . 75% . . . 90% . . . >95%).

The methods of the present invention do not require the hazardous wasteglass to be in a particular form when used as an input material. In someembodiments, hazardous waste glass is used in a granular or powder form.Different powder or grain size can be achieved through various grindingand sieving techniques understood in the art. The glass powder particlesize required depends on the final properties desired. In someembodiments, various types of equipment are used to reduce the particlesize and/or create a powder (e.g., hammer mills, roller mills, androtating pan mixers with Muller-type wheels, etc.). Indeed, any type ofmilling and/or grinding equipment that crushes the agglomerate into apowder can be used for this step. In some embodiments, after crushing,the material is sieved to produce a more uniformly sized flowable powderand/or granulate. Various mesh size sieves (e.g., 10 mesh, 20 mesh, 30mesh, 40 mesh, 50 mesh, 100 mesh, 200 mesh, 400 mesh, 600 mesh, 800mesh, etc.) can be used depending on the powder size desired for theforming process. Particles that do not pass through the sieve can becirculated back to the crushing and/or grinding step.

The present invention is not limited to particular types and/or kinds ofCRT glass. In some embodiments, CRT glass includes, but is not limitedto, panel glass, funnel glass, neck glass, and solders glass. Panelglass or screen glass makes up, for example, the front of the CRT andgenerally accounts for approximately two-thirds of the CRT mass. Panelglass typically contains low concentrations of lead. The funnel is therear portion of the CRT. The funnel is fabricated from leaded glasscontaining up to 28 wt % lead oxide. Most of the lead in the CRT iscontained in the funnel. The neck is the straight glass tube thatsurrounds the electron gun. The neck is also made from leaded glass.Solder glass is used to connect and seal the panel glass to the funnel.The solder glass typically contains concentrations well over 50 wt %lead oxide. A typical CRT contains between 2 and 20 pounds of lead. Dueto the high leaching rate of lead from the CRTs, the EnvironmentalProtection Agency (EPA) has classified CRTs as hazardous waste whendiscarded. The methods of the present invention permit processing CRTglass (e.g., panel glass, funnel glass, neck glass, and solder glass)into ceramic materials and/or products that encapsulate such hazardousmaterials in a safe and non-leaching manner. In some embodiments, themethods of the present invention permit processing of CRT glass withouta need to separate out or discard different regions of the CRT glass(e.g., batch processing).

The present invention is not limited to a particular type of fluorescentlight glass. In some embodiments, fluorescent light glass includes, butis not limited to, fluorescent light bulbs, fluorescent tubes, compactfluorescent lamps, etc. In some embodiments, fluorescent light glasscomprises mercury. In some embodiments, fluorescent light glasscomprises mercury and other toxic and/or heavy metals.

In some embodiments, additional materials (e.g., feldspar) are used asflux materials. For example, in some embodiments, the flux materialcomprises hazardous waste glass and any other suitable flux materials.In some embodiments, additional flux materials include, but are notlimited to, feldspar, ammonium chloride, rosin, zinc chloride, borax,and alkalai metal fluxes (e.g., sodium fluoride, potassium fluoride,etc.).

The present invention is not limited to particular types and/or kinds ofplastic material. In some embodiments, plastic material is clay. Indeed,any suitable clay material finds use as an input material in the presentinvention. In some embodiments, clay is selected as a plastic materialbased on the other input materials (e.g., binder, filler, flux, etc.).In some embodiments, clay is selected as an input material based on thereaction conditions of the methods. In some embodiments, clay isselected as an input material based on the desired characteristics ofthe ceramic product and/or material. Examples of suitable types and/orforms of clays include, but are not limited to, bentonite (e.g., sodiumbentonite, calcium bentonite, potassium bentonite, etc.), kaolinite,smectite (e.g., montmorillonite-smectite), illite, chlorite, derivitiesthereof, and combinations thereof.

The present invention is not limited to particular types and/or kinds offiller. Examples of filler include, but are not limited to, alumina,silica, zirconia titania, ceria, mullite, and silicon carbide. In someembodiments, a filler is selected based on the other input materials(e.g., binder, plastic material, flux, etc.). In some embodiments, afiller is selected as an input material based on the reactionconditions. In some embodiments, a filler is selected as an inputmaterial based on the desired characteristics of the ceramic productand/or material. In some embodiments, the filler comprises alumina,magnesium silicate (e.g., Talc), and/or bentonite (e.g., clay). In someembodiments, the choice of filler is dependent upon the ultimate desireduse of the ceramic article (e.g., indoor/outdoor use for the ceramicarticle) (e.g, use of magnesium silicate as a filler for outdoor ceramicarticles as magnesium silicate withstands temperature changes expansionand contraction

The present invention is not limited to particular types and/or kinds ofbinders. In some embodiments, a binder comprises an alcohol (e.g.,polyvinyl alcohol). In some embodiments, a binder comprises anon-aqueous liquid. Use of a non-aqueous binder in the methods of thepresent invention for generating ceramic products that encapsulatehazardous materials from, for example, hazardous waste glass alleviatesthe need for drying steps within such methods. In some embodiments,binder selection (e.g., selection of a non-aqueous binder, selection ofpolyvinyl alcohol as binder) is a key to generating ceramic articleswhich safely encapsulate hazardous materials (e.g., lead, barium, etc.).In some embodiments, binder selection (e.g., selection of a non-aqueousbinder, selection of polyvinyl alcohol as binder) permits efficient, lowtemperature, environmentally friendly processing of hazardous wasteglass (e.g., CRT glass, fluorescent light glass, etc.). In someembodiments, the non-aqueous binder is sodium silicate. In someembodiments, the non-aqueous binder prevents the emission ofhydrocarbons during, for example, a firing stage (e.g., wherenon-aqueous binder is sodium silicate).

In some embodiments, various additives are added to the input materialsto yield a desired material and/or product (e.g., added strength, color,texture, etc.), or to have a desired effect on the process (e.g., lowerheat, lower pressure, etc.). Common ceramic additives, such asplasticizers, lubricants, colorants, etc. can also be added with theinput materials. In some embodiments, coarse sized particles are addedto adjust properties, such as improving slip resistance by roughing thesurface texture. In some embodiments, addition of any mixtures orcompounds commonly used in the manufacture of ceramic articles,materials, and/or products (e.g., ceramic tiles) is within the scope ofthe present invention.

The methods are not limited to particular percentages of inputmaterials. Indeed, in some embodiments, flux material (e.g., hazardouswaste glass (e.g., CRT glass, fluorescent light glass, etc.)) comprises25-99% of the input materials by weight % (e.g., 25% . . . 35% . . . 45%. . . 55% . . . 65% . . . 75% . . . 85% . . . 95% . . . 99%). In someembodiments, flux material (e.g., hazardous waste glass (e.g., CRTglass, fluorescent light glass, etc.)) comprises at least about 25% ofthe input materials by weight %(e.g., >25%, >35%, >45%, >55%, >65%, >75%, >85%, >95%, etc.). In someembodiments, flux material (e.g., hazardous waste glass (e.g., CRTglass, fluorescent light glass, etc.)) comprises less than about 99% ofthe input materials by weight % (e.g., <99%, <95%, <85%, <75%, <65%,<55%, <45%, <35%, etc.). In some embodiments, a plastic material (e.g.,clay) comprises 5-40% of the input material by weight % (e.g., 5% . . .10% . . . 15% . . . 25% . . . 35% . . . 40%). In some embodiments, aplastic material (e.g., clay) comprises at least about 5% of the inputmaterial by weight % (e.g., >5%, >10%, >15%, >20%, >25%, >30%, >35%,etc.). In some embodiments, a plastic material (e.g., clay) comprisesless than about 40% of the input material by weight % (e.g., <40%, <35%,<30%, <25%, <20%, <15%, <10%, etc.). In some embodiments, a binder(e.g., polyvinyl alcohol or sodium silicate) comprises 0.1-5% of theinput material by weight % (e.g., 0.1% . . . 0.2% . . . 0.5% . . . 1% .. . 2% . . . 3% . . . 4% . . . 5%). In some embodiments, methods of thepresent invention utilize 40-80% flux material (e.g., hazardous wasteglass (e.g., CRT glass)) by wt % of input material. In some embodiments,methods of the present invention utilize 5-40% filler (e.g., alumina) bywt % of input material. In some embodiments, methods of the presentinvention utilize 10-25% plastic material (e.g., clay) by wt % of inputmaterial. In some embodiments, suitable ratios of input materials areprovided in Table 3. In some embodiments, methods of the presentinvention utilize 75-99% (e.g., 85-95%) flux material (e.g., hazardouswaste glass (e.g., CRT glass)) by wt % of input material. In someembodiments, methods of the present invention utilize 1-25% (e.g.,5-15%) filler (e.g., alumina) by wt % of input material.

In some embodiments, the input materials are crushed and/or ground toachieve a desired particulate size or fineness of powder. In someembodiments, material is sieved to produce a more uniformly sizedflowable powder. Particles that do not pass through the sieve can becirculated back to the crushing and/or grinding step.

The present invention is not limited to a particular technique formixing the input materials. In some embodiments, the input materials aremixed to produce a batch mixture by dry stirring, or wet stirringfollowed by a drying procedure. The methods are not limited to aparticular manner of mixing. In some embodiments, input materials aremixed in any type of mixer that will uniformly distribute the components(e.g., pan mixer, conical blender, ribbon mixer, rotating drum mixer,etc.) to yield a batch mixture (e.g., uniform batch mixture,semi-uniform batch mixture). In some embodiments, mixed input materialsare sieved through one or more meshes (e.g., 20 mesh, 40 mesh, 60 mesh,80 mesh, 100 mesh, 150 mesh, 200 mesh, 300 mesh, 400 mesh, etc.), forexample, to eliminate any clumps or particulates.

In some embodiments, the input material (e.g., a flux (e.g., hazardouswaste glass (e.g., CRT glass)), filler (e.g., alumina), and/or plasticmaterial (e.g., clay)) mixture (e.g., batch mixture) is passed through amesh (e.g., 10, mesh, 20 mesh, 40 mesh, 60 mesh, 80 mesh, 100 mesh, 150mesh, 200 mesh, 300 mesh, 400 mesh, etc.) before and/or after mixingwith binder (e.g., polyvinyl alcohol or sodium silicate).

The present invention is not limited to a particular technique forpressing the mixed input materials. In some embodiments, pressing isperformed in a press (e.g., hydraulic press). The pressing is notlimited to a particular degree of pressing. In some embodiments,pressing of the mixed input material is done under at least 50 kg/cm³²(e.g., 50 kg/cm² . . . 100 kg/cm² . . . 200 kg/cm² . . . 300 kg/cm² . .. 400 kg/cm² . . . 500 kg/cm² . . . 750 kg/cm² . . . 1000 kg/cm² . . .2000 kg/cm², etc.). In some embodiments, the mixed input materials arepressed into a desired shape (e.g., a tile) and size (e.g., 1 cm×1 cm, 2cm×2 cm, 3 cm×6 cm, 8 cm×8 cm, 30 cm×30 cm, etc.). In some embodiments,articles (e.g., tiles) of any size (e.g., 1 inch×1 inch, 2 inch×4 inch,3 inch×9 inch, 12 inch×12 inch, 24 inch×24 inch, etc.) and shape (e.g.,square, triangle, circular, ovular, hexagonal, rectangular, etc.) areproduced by pressing the mixed input materials.

In some embodiments, pressing the mixed input material results information of a green article (e.g., green material, green product). Insome embodiments, the pressed green article is allowed to dry for atleast 1 hour (e.g., 1 hour, 2 hours, 4 hours, 12 hours, 24 hours, 2days, 4 days, 1 week, times therein, etc.). In some embodiments, thepressed green article is dried at room temperature (e.g., approximately23° C.) and or in an oven (e.g., 25° C. . . . 40° C. . . . 60° C. . . .80° C. . . . 100° C. . . . 110° C. . . . 150° C. . . . 200° C., etc.).

The present invention is not limited to a particular technique forfiring the green article resulting from pressing of the mixed inputmaterial. In some embodiments, the green article is fired (e.g., in akiln, furnace, or oven) at temperatures ranging from 500-2000° C. (e.g.,500° C., 600° C., 700° C., 800° C., 900° C., 1000° C., 1200° C., 1400°C., 1600° C., 1800° C., 2000° C., temperatures therein, etc.). In someembodiments, the green article is fired (e.g., in a kiln, furnace, oroven) at a temperature not exceeding 2000° C. (e.g., <1800° C., <1600°C., <1400° C., <1200° C., <1000° C., <800° C., etc.). In someembodiments, firing is performed on a fast firing schedule (e.g., 45minutes, 60 minutes 2 hours, etc.) or a slow firing schedule (e.g., 8hours, 12 hours, 24 hours, etc.). In some embodiments, a green articleis fired for at least 15 minutes (e.g., >15 minutes, >30 minutes, >60minutes, >2 hours, >4 hours, >6 hours, >8 hours, >10 hours, >12hours, >24 hours, etc.) to yield a ceramic article.

Experiments conducted during the course of developing embodiments forthe present invention determined that the required firing temperature togenerate a ceramic product is varies inversely with the weight percentof flux material (e.g., hazardous waste glass (e.g., CRT glass,fluorescent light glass, etc.)). For example, it was shown that ceramicloaded with up to 70 wt % CRT glass can be produced at around 1000° C.with negligible shrinkage (e.g., <0.5%), warpage or bending. Inaddition, it was shown that ceramic with a lower loading of CRT glassrequires higher firing temperatures for sintering (e.g., up to 1250°C.). Experiments further demonstrated that ceramic with approximately95% flux material (e.g., hazardous waste glass (e.g., CRT glass,fluorescent light glass, etc.) was fired with a heating rate of 100° C.per hr to 670° C.; ceramic with approximately 92.5% flux material (e.g.,hazardous waste glass (e.g., CRT glass, fluorescent light glass, etc.)was fired to approximately 705° C.; ceramic with approximately 85% fluxmaterial (e.g., hazardous waste glass (e.g., CRT glass, fluorescentlight glass, etc.) was fired to approximately 815° C. Accordingly, itwas determined that higher loadings of CRT glass allow for substantiallyreduced maximum firing temperatures. Indeed, ceramic loaded with 80 and90% CRT glass reduced the maximum firing temperature to around 830° C.and 700° C., respectively. As such, it was determined that increasingthe wt % of hazardous waste glass (e.g., CRT glass, fluorescent lightglass, etc.) results in 1) increased recycling efficiency (e.g., amountof waste material recycled per production run), 2) increased amount oftoxic metal encapsulation, and 3) decreased energy requirements throughreduction of required firing temperature.

The methods of the present invention generate ceramic articlescomprising significant quantities of hazardous materials that are safelyencapsulated and/or configured to prevent leaching of hazardousmaterials. In some embodiments, the hazardous materials include, but arenot limited to, heavy metals (e.g., mercury, arsenic, cadmium, cobalt,chromium, copper, manganese, nickel, lead, tin, thallium, etc.) and/ortoxic metals (e.g., antimony, barium, beryllium, aluminum, cadmium,lead, mercury, osmium, thallium, and vanadium. In some embodiments, theceramic articles comprise significant quantities of lead(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). In some embodiments, the ceramic articles comprise significantquantities of barium(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). In some embodiments, the ceramic articles comprise significantquantities of cadmium(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). In some embodiments, the ceramic articles comprise significantquantities of mercury(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). In some embodiments, the ceramic articles comprise significantquantities of silver(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). In some embodiments, the ceramic articles comprise significantquantities of selenium(e.g., >0.1%, >0.2%, >0.5%, >1.0%, >2.0%, >5.0%, >10%, >20%, >50%,etc.). The ceramic articles comprising significant quantities ofhazardous materials that are safely encapsulated and/or configured toprevent leaching of hazardous materials meet or exceed EnvironmentalProtection Agency (EPA) standards for toxicity and leaching (e.g.,leaching of toxic and/or heavy metals). For example, ceramic articles ofthe present invention meet or exceed Environmental Protection Agency(EPA) standards when subjected to the Toxicity Characteristic LeachingProcedure (TCLP). In some embodiments, ceramic articles of the presentinvention exhibit TCLP barium leachate concentrations less than 100 ppm(e.g., <50 ppm, <20 ppm, <10 ppm, <5 ppm, etc.). In some embodiments,ceramic articles of the present invention exhibit TCLP lead leachateconcentrations less than 5 ppm (e.g., <5 ppm, <4 ppm, <3 ppm, <2 ppm, <1ppm, <0.5 ppm, <0.1 ppm, etc.). In some embodiments, ceramic articles ofthe present invention exhibit TCLP cadmium leachate concentrations lessthan 1 ppm (e.g., <1 ppm, <0.5 ppm, <0.1 ppm, <0.05 ppm, etc.). In someembodiments, ceramic articles of the present invention exhibit TCLPmercury leachate concentrations less than 0.2 ppm (e.g., <0.2 ppm, <0.1ppm, <0.05 ppm, <0.02 ppm, <0.01 ppm, etc.). In some embodiments,ceramic articles of the present invention exhibit leachateconcentrations for all hazardous monitored organic and inorganicanalytes (SEE Table 1).

TABLE 1 Maximum Concentration of Contaminants for ToxicityCharacteristic Contaminant Regulated Level (ppm) Arsenic (As) 5.0 Barium(Ba) 100 Benzene 0.5 Cadmium (Cd) 1.0 Carbon Tetrachloride 0.5 Chlordane0.03 Chlorobenzene 100 Chloroform 6.0 Chromium (Cr) 5.0 o-Cresol 200m-Cresol 200 p-Cresol 200 Cresol 200 2,4-Dichlorophenoxyacetic acid 101,4-Dichlorobenzene 7.5 1,2-Dichloroethane 0.5 1,1-Dichloroethylene 0.72,4-Dinitrotoluene 0.13 Endrin 0.02 Heptachlor 0.008 Hexachlorobenzene0.13 Hexachlorobutadiene 0.5 Hexachloroethane 3.0 Lead (Pb) 5.0 Lindane0.4 Mercury (Hg) 0.2 Methoxychlor 10 Methyl ethyl ketone 200Nitrobenzene 2.0 Pentachlorophenol 100 Pyridine 5.0 Selenium (Se) 1.0Silver (Ag) 5.0 Tetrachloroethylene 0.7 Toxaphene 0.5 Trichloroethylene0.5 2,4,5-Trichlorophenol 400 2,4,6-Trichlorophenol 2.0 2,4,5-TP(Silvex) 1.0 Vinyl Chloride 0.2

In some embodiments, ceramic articles of the present invention exhibitstructural characteristics on par with, or superior to, similarconventional articles (i.e. not manufactured from hazardous waste glassand/or by the methods of the present invention). In some embodiments,ceramic articles of the present invention exhibit thermal shockresistance comparable to similar conventional ceramic articles, do notexhibit warpage or exhibit negligible warpage (e.g., <5%, <2%, <1%,<0.5%, <0.1%). In some embodiments, ceramic articles of the presentinvention exhibit breaking strengths comparable to similar conventionalceramic articles. In some embodiments, ceramic articles of the presentinvention exhibit breaking strengths superior to similar conventionalceramic articles. In some embodiments, ceramic articles of the presentinvention exhibit high chemical resistance. In some embodiments, ceramicarticles of the present invention are highly resistant to freeze damage.In some embodiments, ceramic articles of the present invention arehighly resistant to abrasion. In some embodiments, ceramic articles ofthe present invention are highly resistant to staining. In someembodiments, ceramic articles of the present invention are highlyresistant to color fading. In some embodiments, ceramic articles of thepresent invention are highly resistant to loss of texture and/or texturefading.

In some embodiments, methods of the present invention find utility withother conventional ceramic production (e.g., ceramic tile production)procedures (e.g., single firing, double firing, glazing, etc.). In someembodiments, methods of the present invention are used with methods forproviding decoration to ceramic articles (e.g., glazing, coloring,patterning, etc.).

EXPERIMENTAL Example 1 Scheme 1 Conventional Processing

Preparation of Ceramic Tiles by Conventional Ceramic ProcessingTechniques and the desired properties of such tiles are described in theAmerican National Standard Specifications for Ceramic Tiles (ANSIA137.1), published by the Tile Council of America (TCA). Tiles can beglazed or unglazed, and the performance requirements vary depending uponthe application. In conventional tile compositions the ratio offlux:filler:plastic is generally 20:20:60. Experiments were performedduring development of embodiments of the present invention to establishcompositions and methods to produce a ceramic product using CRT glassprimarily as a fluxing material. CRT glass begins to flow at arelatively low temperature (around the glass transition point) and is ofcomparable composition to that of the natural fluxing mineral feldspar(SEE Table 2).

TABLE 2 Chemical Composition of Feldspar and CRT Glass (wt %). OxideFeldspar CRT glass SiO₂ 67.97 61.29 BaO 0.133 10.70 Na₂O 7.39 8.92 K₂O4.74 7.47 PbO 0 5.05 SrO 0.042 2.40 Al₂O₃ 18.27 2.08 CaO 1.4 0.65 ZrO₂ 00.43 Sb₂O₃ 0 0.33 F 0 0.30 CeO₂ 0 0.16 Fe₂O₃ 0 0.15 MgO 0 0.14 TiO₂ 00.11 ZnO 0.001 0.10 CuO 0 0.01However, adherence to the typical 20-25% limit for fluxing materialwould likely produce inefficient (e.g., economically inefficient,environmentally inefficient, etc.) CRT loadings. Experiments wereperformed during development of embodiments of the present invention todetermine the maximum achievable waste loading in the CRT-based ceramictile, based on modifications of the standard tile manufacturing methods.

The properties of the fired ceramic tile body were examined as functionsof waste loading (e.g., 40 to 80 wt % of CRT glass) and firing schedule(e.g., different maximum temperature (e.g., 650° C. to 1250° C.),different time durations at maximum temperature). Clay was selected asthe plastic material and alumina was used as the filler, in addition tothe CRT glass. The weighed ingredients were mixed by wet stirring anddried in an oven at 110° C. The dried batch was sieved through 100 mesh,then sieved through 20 mesh after being mixed with the binder material.The resulting material was pressed into a 2″×2″ tile in a uniaxial pressat 400 kg/cm² pressure. After pressing, tiles were dried in an oven at110° C. for at least 48 hours. The tiles were then fired at differenttemperatures, ranging from 650-1250° C. with two hours soaking,depending on the compositions (SEE FIG. 1). The firing of the tiles wasdone using slow or fast schedules. The ingredients of the CRT-basedtiles are summarized in Table 3. Coloring agents were added to selectedtiles to produce single-fired colored tiles.

TABLE 3 Batch Composition of Tile Body Utilizing CRT Glass (wt %). CRTglass powder 40 50 60 70 80 Filler (alumina) 30-40 20-30 20-25 15-20 5-10 Kaolin and Ball clay 15-20 20-25 15-20 10-15 10-15

The overall appearance of the fired ceramic tiles is demonstrated by thescanned images shown in FIG. 2, which were obtained using an opticalscanner. Crystalline phase identification analysis by X-ray diffraction(XRD) was performed on powdered samples of the fired tiles.Microstructures were examined using scanning electron microscopy coupledwith energy dispersive x-ray spectroscopy (SEM/EDS). Water absorptionwas measured using the American Society for Testing and Materials (ASTM)procedure [7]. The toxicity characteristic leaching procedure (TCLP)response of the fired tile was also measured following the US EPA Method1311 protocol.

Experiments conducted during development of embodiments of the presentinvention demonstrated that ceramic tiles of good quality can be madefollowing the standard tile industrial method while incorporating veryhigh percentages of CRT glass (SEE Table 4).

TABLE 4 Observed Fired Properties of Ceramic Tiles Made from CRT Glass.Tile name T12 T16 T18 T19 T20 T22 CRT loading 40% 50% 60% 70% 80% 90%Temperature 1150-1250 1150-1250 1050-1250 900-1030 <830 <750 tested forsintering, ° C. Shrinkage, % No shrinkage No shrinkage No shrinkage Noshrinkage ~4 ~4 Warpage No warpage No warpage No warpage No warpageBending Bending observed observed Water 3 7 4 0.2 Not done No doneabsorption. % (for 1250° C.) (for 1150° C.) (for 1250° C.) (for 950° C.)Structure Porous Porous Porous Semivitreous Semivitreous Semivitreous

A ceramic tile loaded with as high as 70 wt % CRT glass can be producedat around 1000° C. following a fast firing schedule with negligibleshrinkage (<0.5%) and warpage or bending. The tiles with a lower loadingof CRT glass required higher temperatures for sintering, up to 1250° C.Higher loadings of CRT glass reduced the maximum firing temperaturesubstantially. Tiles loaded with 80 and 90% CRT glass further reducedthe maximum firing temperature to around 830 and 700° C., respectively.However, at 80-90% loading, shrinkage and bending became noticeable forthe test samples. CRT glass produced ceramic tile with a brilliantoff-white color after firing and minimum dimensional shrinkage andwarpage for wide ranges of glass loading (SEE FIG. 2). The distinctivebrilliant whitish color of the CRT tile makes it very amenable toattractive coloration for decoration purposes. Dimensional stability isvery important for wall tiles, for which there is only 1% shrinkagetolerance, and floor tiles which have a maximum 3-4% shrinkagetolerance. Visual inspection of the CRT tiles generally reported highlydesirable brilliant off-white color with virtually zero shrinkage andwarpage. The color of the tiles varies with loading of CRT glass alongwith firing temperature in some cases. The corners of the tiles werefound to be very sharp. Empirical chipping and impacting tests indicatedthat the tiles were very hard and would exhibit good flexural strength.CRT tiles of a wide range of compositions all showed exceptional toacceptable water absorption (See Table 5).

TABLE 5 Water Absorption Results for Tiles made from CRT Glass. Waterabsorption. % 40% loading 50% loading 60% loading 70% loading 1250° C.3% Not done 4% Not done 1150° C. Not done 7% Not done Not done 1050° C.Not done Not done Not done   0%  950° C. Not done Not done Not done 0.2%

The microstructures of selected tile samples were examined by SEM. Theresults show a porous texture. With increasing glass content, thevitreous phase fraction tends to increase, which in turn results in adenser and less porous ceramic body. Most pores, as shown by opticalmicroscopy and SEM, were closed in nature and the shapes of the poreswere nearly round. The higher magnification SEM images show developmentof some needle-shaped crystalline phases surrounding the fillermaterials, which appeared to have grown at the expense of the vitreousphase (SEE FIG. 3). EDS analysis of the acicular phases indicate thepresence of high contents of barium, potassium, aluminum, and silicon,suggesting an aluminosilicate phase resembling barium-bearing feldspar.Indeed, the XRD powder patterns of the same tile sample, with 60 wt %CRT, identify two major crystalline phases, corundum and hyalophane, andminor amounts of mullite (SEE FIG. 4). Hyalophane is a potassium-bariumaluminosilicate that tends to be needle-like.

The TCLP leach test was performed on tiles with 40 wt % CRT loading. Theresults showed TCLP leachate concentrations of 1.29 ppm for Ba and 0.38ppm for Pb (SEE Table 6); these are well below the EPA TCLP limits of100 ppm and 5 ppm, respectively.

TABLE 6 Results of TCLP Testing Tiles Made from CRT Glass. Sample Ba(ppm) Pb (ppm) Sr (ppm) T12 (40% CRT) 1.29 0.38 0.22

Example 2 Scheme 2 Powder-Sintering

Ceramic tiles were prepared using high CRT glass loadings of 85-95 wt %by sintering the powdered waste glass with Al₂O₃ as a filler material.This technique is referred to as the “powder-sintering” method of tileprocessing. Ground CRT waste glass was mixed with 5-15% alumina anddry-pressed with the addition of polyvinyl alcohol as a binder forimproving green strength. Both CRT waste glass and alumina are highlynonplastic. Addition of water to the powdered batch was avoided,therefore the drying operation was not required. Fully sintered anddense tiles were obtained after firing at relatively low temperatures inthe range 650-815° C.

Synthesized CRT glass of the average composition shown in Table 1 wasused for ceramic tile production. In addition, funnel, faceplate, andneck glasses from an actual CRT [5] were utilized in some tilepreparations. The CRT glass was broken with a hammer and then groundusing mortar and pestle until the material passed a 200-mesh sieve. Thecomposition of the glass mixture as determined by XRF is given in Table7.

TABLE 1 Reference Average CRT Glass Composition (Target) [6] and XRFAnalysis of Synthesized Material Used in This Work (wt %). Oxide TargetXRF SiO₂ 60.92 61.29 BaO 10.80 10.70 Na₂O 8.96 8.92 K₂O 7.44 7.47 PbO5.02 5.05 SrO 2.39 2.40 Al₂O₃ 2.07 2.08 CaO 0.67 0.65 ZrO₂ 0.43 0.43Sb₂O₃ 0.33 0.33 F 0.30 0.30 CeO₂ 0.16 0.16 Fe₂O₃ 0.15 0.15 MgO 0.14 0.14TiO₂ 0.11 0.11 ZnO 0.10 0.10 CuO 0.01 0.01

TABLE 7 CRT Glass Composition. Oxide Wt % SiO₂ 57.57 Na₂O 8.01 BaO 7.49K₂O 7.33 SrO 7.33 PbO 4.69 Al₂O₃ 2.00 CaO 1.87 ZrO₂ 1.69 MgO 0.76 TiO₂0.36 Sb₂O₃ 0.36 CeO₂ 0.30 Fe₂O₃ 0.06 SO₃ 0.04 HfO₂ 0.04 IrO₂ 0.03 ZnO0.02 Pr₅O₁₁ 0.01 O₅O₄ 0.0114 SnO₂ 0.0056 CuO 0.0052 Cr₂O₃ 0.0043 NiO0.0041 Rb₂O 0.0035

Alumina was added in the appropriate amount and mixed, first by shakingthe blend in a plastic container, followed by mechanical mixing in ahigh-speed blender. Polyvinyl alcohol (1 wt %) was added to the mixedpowder as a binder. The mixture was then placed in a 10-MT hydraulicpress to form the green tile. The green tile samples were fired in afurnace with a heating rate of 100° C. per hr to 670° C. for the 5%alumina sample; 705° C. for the 7.5% alumina sample; and 815° C. for the15% alumina sample.

Tiles were made via the powder-pressing method with aluminaconcentrations between 5 and 15 wt %. Samples were subjected to TCLPleach testing. Tiles made with 5 wt % and 7.5 wt % alumina gave TCLPbarium leachate concentrations of 5.17 ppm and 5.86 ppm, respectively,and lead leachate concentrations of 3.45 and 3.69 ppm, respectively.These values are below the EPA TCLP limits of 100 ppm and 5 ppm,respectively. Improvements in TCLP leachability are possible byoptimizing the CRT waste loadings and additives.

The principal crystalline phase identified in the samples by XRD wasNa-Kanorthite. However, the XRD patterns also indicate the presence of asubstantial fraction of glassy phase in the tiles (SEE FIG. 5).

Ceramic containing 15 wt % alumina is much lighter in color than sampleswith lower alumina content. All samples were able to be polished to avery glossy finish on account of the high glass content in these tiles.The finish was achieved without glaze coating.

The waste-tiles prepared by the powder-processing method are strong andtough compared to the tiles currently marketed. The large fraction ofglassy phase resulted in minimal porosity. Tiles can be produced by thisroute in almost any dimension and color.

The overall economic feasibility of processing CRT glass wastes, intotiles by the powder-processing method (e.g., mixing with a modest amountof a filler compound (e.g., alumina) and firing the green tiles atmoderate temperatures) is both more economically attractive andtechnologically simpler than the traditional ceramic or glass-ceramicroutes. The filler material can alternatively be from a range of wasteproducts from the ceramic/refractories industries, such as firedrefractory and pottery wastes (grog) of almost any composition, insteadof alumina. The disposal of fired ceramic wastes is often a problem forthese industries. Accordingly, the filler grog may be procured cheaplyor may even with compensation. Conventional tile manufacturingnecessitates the sintering temperature to be around 1250-1400° C. Atsuch high temperatures, a reduction of sintering temperature by 100° C.reduces the energy cost by almost 50%. The energy savings between firingceramic bodies at 1350° C. and 815° C. is conservatively estimated at65% if the low temperature route is adopted. Considering that almost 50%of the processing cost in ceramic industries comprises energyexpenditures, this could represent a further competitive edge for CRTtiles. In the powder processing method, several unit operations such ascrushing, grinding, and sieving/grading of clay, quartz, and feldsparwill be avoided. Crushing and grinding hard minerals such as quartz andfeldspar are the second most energy-intensive operations in the ceramicindustry. In the powder sintering route, these operations will besubstituted by crushing/grinding grog, which will compose only 5-15% ofthe final product as compared to 40-60% for the traditional ceramicprocessing route. This will save, for example, an additional 10% of theenergy usage. Slip preparation will not be required in this process. Itis estimated that an additional 10-15% savings in energy could berealized by avoiding this operation. The savings in man-powerrequirements by avoiding the traditional unit operations used inconventional tile manufacturing could be as much as, for example, 50%.

The results obtained in experiments conducted during development of thepresent invention demonstrate that high loadings of CRT waste glass canbe used in the fabrication of ceramic tiles using a relatively simpledry pressing and low-temperature sintering method. This process utilizesthe favorable amorphous (glassy) properties of the CRT waste glasses toreduce processing costs apparently without compromising any of the vitalcharacteristics required of a wall or floor tile.

Example 3 Scheme 3 Glass Ceramic

Glass-ceramic processing was conducted by first melting simulated CRTwaste glass with additives consisting of 2-10 wt % P₂O₅ and TiO₂. P₂O₅and TiO₂ are known nucleating agents and are added to glass batchesduring the processing of glass-ceramic products. Typical glass batchescontaining the two additives had high melting temperatures (˜1550° C.)and the melt exhibited very poor flow properties. However, the glassescrystallized fairly homogeneously at nucleation and growth temperaturesin the range of 700-850° C. Relatively tough glass-ceramic tiles wereprepared by this method.

All publications and patents mentioned in the above specification areherein incorporated by reference. Various modifications and variationsof the described method and system of the invention will be apparent tothose skilled in the art without departing from the scope and spirit ofthe invention. Although the invention has been described in connectionwith specific preferred embodiments, it should be understood that theinvention as claimed should not be unduly limited to such specificembodiments. Indeed, various modifications of the described modes forcarrying out the invention that are obvious to those skilled in therelevant fields are intended to be within the scope of the followingclaims.

REFERENCES

-   [1] “State of the U.S. Ceramic Tile Industry (Fall 2001),” presented    by Robert E. Daniels, published in newsletter of The Tile Council of    America; herein incorporated by reference in its entirety.-   [2] “Testing of Recycled Glass and Inorganic Binder Paving    Tiles—Final Report,” (Report no. GL-99-2), University of Washington,    May 1999; herein incorporated by reference in its entirety.-   [3] “Creating Markets for Recycled Resources—Materials Recovery from    Waste Cathode Ray Tubes (Project Code GLA15-006),” written by ICER    (Industry Council for Electronic Equipment Recycling), published by    The Waste & Resources Action Programme, November 2003; herein    incorporated by reference in its entirety.-   [4] “Potential Markets for CRTs and Plastics from Electronics    Demanufacturing: An Initial Scoping Report—Technical Report #6,”    Chelsea Center for Recycling and Economic Development, University of    Massachusetts, August 1998, Chelsea, Mass.; herein incorporated by    reference in its entirety.-   [5] “Analysis and Leach Testing of CRT Glasses,” R. K. Mohr    and I. L. Pegg, VSL-04R4390-1, Rev. 0, Vitreous State Laboratory,    The Catholic University of America, Washington, D.C., May 25, 2004;    herein incorporated by reference in its entirety.-   [6] “GW-12.10-130: New Approach to Cathode Ray Tube (CRT)    Recycling,” Industry Council for Electronic Equipment Recycling,    Prepared for the Department of Trade and Industry, (UK) August 2003;    herein incorporated by reference in its entirety.-   [7] “Standard Test Method for Water Absorption, Bulk Density,    Apparent Porosity and Apparent Specific Gravity of Fired Whiteware    Products,” ASTM C373-88 (reapproved 1999); herein incorporated by    reference in its entirety.-   [8] “Characterization of Lead Leachability from Cathode Ray Tubes    Using the Toxicity Characteristic Leaching Procedure,” T. G.    Townsend, S. Musson, Yong-Chul Jang, Il-Hyun Chung, Report to    Florida Center for Solid and Hazardous Waste Management, State    University System of Florida, Gainesville, Fla., December 1999;    herein incorporated by reference in its entirety.-   [9] “Fabrication of Ceramic Tiles from Waste CRT Glass,” M.    Chaudhuri, B. Dutta, T. Barnard, H Gan, and I. Pegg, VSL-05R5390-1,    Rev. 0, Vitreous State Laboratory, The Catholic University of    America, Washington, D.C., Jan. 18, 2005; herein incorporated by    reference in its entirety.

1. A method of producing a ceramic article from hazardous waste glasscomprising: a) mixing hazardous waste glass with a filler and anon-aqueous binder; b) pressing the mixture to produce a green article;and c) firing said green article to produce a ceramic article.
 2. Themethod of claim 1, wherein said hazardous waste glass comprises one ormore of the following characteristics: greater than 1% lead, greaterthan 5% lead, greater than 20% lead, CRT glass, fluorescent light glass,greater than 1% barium, greater than 5% barium, and greater than 20%barium.
 3. The method of claim 2, wherein said filler is selected fromthe group consisting of alumina, magnesium silicate, and bentonite. 4.The method of claim 1, wherein said non-aqueous binder is selected fromthe group consisting polyvinyl alcohol and sodium silicate.
 5. Themethod of claim 1, wherein pressing is selected from the groupconsisting of dry pressing, placing the mixture under pressure of atleast 200 kg/cm², and placing the mixture under pressure of about 400kg/cm².
 6. The method of claim 1, wherein said firing is selected fromthe group consisting of heating said green article to at least 500° C.,heating said green article to a temperature less than 1000° C., heatingsaid green article to at least 650° C., heating said green article to atemperature less than 815° C.
 7. The method of claim 1, wherein saidceramic article comprises one or more of the following characteristics:safely encapsulates the hazardous components of said hazardous wasteglass, meets EPA standards for toxicity and leaching of said toxicand/or heavy metals, exhibits lead leachate concentrations of less than5 ppm, exhibits barium leachate concentrations of less than 100 ppm, andexhibits barium leachate concentrations of less than 10 ppm.
 8. A methodof producing a ceramic article from hazardous waste glass comprising: a)mixing hazardous waste glass with a filler and a plastic material; b)mixing the hazardous waste glass, filler, and plastic material mixturewith a non-aqueous binder to produce a batch mixture; c) pressing saidbatch mixture to produce a green article; d) drying the green article;and e) firing the green article to produce a ceramic article.
 9. Themethod of claim 8, wherein said hazardous waste glass comprises one ormore of the following characteristics: greater than 1% lead, greaterthan 5% lead, greater than 20% lead, CRT glass, fluorescent light glass,greater than 1% barium, greater than 5% barium, and greater than 20%barium.
 10. The method of claim 8, wherein said filler is selected fromthe group consisting of alumina, magnesium silicate, and bentonite,wherein said plastic material comprises clay, and wherein saidnon-aqueous binder is selected from the group consisting polyvinylalcohol and sodium silicate.
 11. The method of claim 8, wherein mixingsaid hazardous waste glass with said filler and said plastic materialcomprises wet stirring followed by drying.
 12. The method of claim 8,wherein pressing is selected from the group consisting of dry pressing,placing the mixture under pressure of at least 200 kg/cm², and placingthe mixture under pressure of about 400 kg/cm².
 13. The method of claim8, wherein said firing is selected from the group consisting of heatingsaid green article to at least 500° C., heating said green article to atemperature less than 1400° C., heating said green article to at least650° C., heating said green article to a temperature less than 1250° C.14. The method of claim 8, further comprising a step between steps (a)and (b) of sieving said batch mixture through a first mesh, wherein saidfirst mesh comprises a 50-150 mesh; further comprising a step betweensteps (b) and (c) of sieving said batch mixture through a second mesh,wherein said second mesh comprises a 10-40 mesh.
 15. The method of claim8, wherein said ceramic article comprises one or more of the followingcharacteristics: safely encapsulates the hazardous components of saidhazardous waste glass, meets EPA standards for toxicity and leaching ofsaid toxic and/or heavy metals, exhibits lead leachate concentrations ofless than 5 ppm, exhibits barium leachate concentrations of less than100 ppm, and exhibits barium leachate concentrations of less than 10ppm.
 16. A composition comprising a ceramic article comprising hazardouswaste glass.
 17. The ceramic article of claim 16, wherein said ceramicarticle is selected from the group consisting of a ceramic tile, a floortile, and a wall tile.
 18. The ceramic article of claim 16, wherein saidhazardous waste glass comprises one or more of the followingcharacteristics: greater than 1% lead, greater than 5% lead, greaterthan 20% lead, CRT glass, fluorescent light glass, greater than 1%barium, greater than 5% barium, and greater than 20% barium.
 19. Theceramic article of claim 16, wherein said hazardous waste glasscomprises fluorescent light glass.
 20. The ceramic article of claim 16,wherein said ceramic article comprises one or more of the followingcharacteristics: greater than 40% hazardous waste glass, greater than60% hazardous waste glass, greater than 80% hazardous waste glass,greater than 90% hazardous waste glass, safely encapsulates thehazardous components of said hazardous waste glass, meets EPA standardsfor toxicity and leaching of said toxic and/or heavy metals, exhibitslead leachate concentrations of less than 5 ppm, exhibits bariumleachate concentrations of less than 100 ppm, and exhibits bariumleachate concentrations of less than 10 ppm.